Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_213606.3 | 1544 | Missense Mutation | TCT,TTT | S452F | NP_998771.3 |
XM_017016237.1 | 1544 | Missense Mutation | TCT,TTT | S452F | XP_016871726.1 |
XM_017016238.1 | 1544 | Missense Mutation | TCT,TTT | S452F | XP_016871727.1 |
XM_017016239.1 | 1544 | Missense Mutation | TCT,TTT | S452F | XP_016871728.1 |